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Gene entry

DNAH1

dynein axonemal heavy chain 1

Chromosome
3
Cytoband
3p21.1
Variants (rsID)
45

DNAH1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.1). Its official name is “dynein axonemal heavy chain 1”. The reference table lists 45 variants (rsID) for this gene.

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Clinically classified variants

26 reference-table entries with clinical significance.

  • rs138320093Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs144580984Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs17052095Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs17052097Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs200859252Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs419752Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs61731638Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs61734631Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs61734638Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs61734644Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37|Premature ovarian insufficiency
  • rs61739896Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs73072968Benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs199602894Conflicting interpretationssingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs138940904Likely benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs181919231Likely benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs185397176Likely benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs202174386Likely benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs61734629Likely benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs79689614Likely benignsingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs140883175Uncertain significancesingle nucleotide variantSpermatogenic failure 18|Spermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs143443167Uncertain significancesingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37|Primary ciliary dyskinesia
  • rs185905489Uncertain significancesingle nucleotide variantCiliary dyskinesia, primary, 37|Spermatogenic failure 18
  • rs188851585Uncertain significancesingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37
  • rs192723261Uncertain significancesingle nucleotide variantCiliary dyskinesia, primary, 37|Spermatogenic failure 18
  • rs77451372Uncertain significancesingle nucleotide variantSpermatogenic failure 18|Ciliary dyskinesia, primary, 37|Primary ciliary dyskinesia
  • rs61734640Not classifiedmissense_variantOsteoarthritis

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.